| | EDRF1-AS1, EDRF1-DT +1036 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126861107, LOC128598885 +802 more | Copy number gain | See cases | |
| | ABLIM1, ABRAXAS2 +679 more | Copy number gain | See cases | |
| | ABRAXAS2, ACADSB +514 more | Copy number gain | See cases | |
| | LOC130004884, LOC130004885 +438 more | Copy number gain | See cases | |
| | LOC130004881, LOC130004882 +418 more | Copy number loss | See cases | |
| | LOC130005014, LOC130005015 +409 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC130004911, LOC130004912 +395 more | Copy number loss | See cases | |
| | ABRAXAS2, ACADSB +383 more | Copy number loss | See cases | |
| | ABRAXAS2, ACADSB +164 more | Copy number loss | See cases | |
| | LOC130004994, LOC130004995 +361 more | Copy number loss | See cases | |
| | ABRAXAS2, ACADSB +182 more | Copy number loss | See cases | |
| | ABRAXAS2, ADAM12 +331 more | Copy number loss | See cases | |
| | ABRAXAS2, ADAM12 +318 more | Copy number loss | See cases | |
| | ABRAXAS2, ADAM12 +318 more | Copy number loss | See cases | |
| | ABRAXAS2, ADAM12 +311 more | Copy number loss | See cases | |
| | ABRAXAS2, ADAM12 +117 more | Copy number gain | See cases | |
| | ABRAXAS2, ADAM12 +297 more | Copy number loss | See cases | |
| | LOC130005026, LOC130005027 +257 more | Copy number loss | See cases | |
| | | Duplication | not specified | |
| | LOC126861090, LOC126861091 +250 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (nonsense +1 more) | See cases | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EDRF1, EDRF1-AS1 (E838K +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EDRF1, EDRF1-AS1 (T906M +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EDRF1, EDRF1-AS1 (R926P +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EDRF1, EDRF1-AS1 (G899A +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EDRF1, EDRF1-AS1 (N937Y +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EDRF1, EDRF1-AS1 (Y1034C +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | EDRF1, EDRF1-AS1 (V1008F +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | EDRF1, EDRF1-AS1 (H1012N +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number loss | not specified | |
| | ABLIM1, ABRAXAS2 +117 more | Copy number gain | not provided | |
| | ABLIM1, ABRAXAS2 +145 more | Copy number gain | Distal trisomy 10q | |
| | | Copy number loss | Distal 10q deletion syndrome | |
| | | Copy number gain | Distal trisomy 10q | |
| | | Copy number loss | Distal 10q deletion syndrome | |
| | ABRAXAS2, CHCHD1 +673 more | Copy number loss | Distal 10q deletion syndrome | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not specified | |
| | ABLIM1, ABRAXAS2 +146 more | Copy number gain | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | See cases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | ABLIM1, ABRAXAS2 +130 more | Copy number gain | not provided | |
| | ABLIM1, ABRAXAS2 +146 more | Copy number gain | not provided | |
| | | Copy number gain | not provided | |